The present invention is generally directed to an agricultural formulation comprising, ethaboxam, metalaxyl and a compound selected from the group consisting of 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide and mandestrobin, a process for preparing the agricultural formulation and methods of use thereof.
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6. A process for preparing an agricultural formulation comprising ethaboxam, metalaxyl and a compound selected from the group consisting of 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide and mandestrobin comprising the steps of:
bead milling ethaboxam and the compound selected from the group consisting of 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide and mandestrobin to create a mill base;
adding metalaxyl to propylene glycol and stirring to create a metalaxyl solution; and
adding the metalaxyl solution to the mill base while agitating to create the agricultural mixture, wherein w/w denotes weight by total weight of the formulation.
3. An agricultural formulation comprising:
about 3.13% w/w mandestrobin;
about 2.35% w/w ethaboxam;
about 1.25% w/w metalaxyl;
about 34.04% w/w propylene glycol;
about 7.33% w/w of a colorant dispersant;
about 0.065% w/w methyloxirane polymer;
about 0.26% or 1.26% w/w of a sodium salt of naphthalene sulfonate condensate;
about 0.065% w/w of a mixture of sodium salt of alkyl vinyl ether/maleic acid half-ester copolymer and polyvinyl pyrrolidone;
about 0.026% w/w of a silicone emulsion;
about 0.3% w/w xanthan gum;
about 0.24% w/w 1, 2-benzisothiazolin-3-one prepared at a concentration of 19.3%;
about 1.0% or 3.0% w/w polyoxyethylene tristyrylphenol phosphate, potassium salt;
about 2.5% w/w carnauba wax; and
optionally, about 1.0% w/w alkylphenol ethoxylate free nonionic wetter and dispersant package,
wherein w/w denotes weight by total weight of the formulation.
1. A stable agricultural formulation comprising:
about 5.3% w/w ethaboxam:
about 2.8% w/w metalaxyl;
about 3.5% w/w 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide;
about 43% w/w propylene glycol;
water;
from about 1.9% to about 2.5% w/w methyloxirane polymer;
about 0.2% w/w of a sodium salt of naphthalene sulfonate condensate;
from about 0.5% w/w to about 0.7% w/w a mixture of sodium salt of alkyl vinyl ether/maleic acid half-ester copolymer and polyvinyl pyrrolidone;
about 0.02% w/w of a silicone emulsion; and
from about 0.12% to about 0.24% w/w of a first component comprising about 19.3% w/w of 1, 2-benzisothiazolin-3-one, wherein w/w of 1,2-benzisothiazolin-3-one denotes weight by total weight of the first component,
wherein w/w denotes weight by total weight of the composition formulation unless otherwise indicated.
4. A method of protecting plants comprising treating plant propagation material with a fungicidally effective amount of the product of
5. A method for controlling or preventing pest damage of plants comprising applying to the plant propagation material an effective amount of the product of
7. The process of
8. The process of
9. The process of
10. The process of
11. The process of
12. The process of
14. The process of
15. The process of
16. The process of
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The present invention is generally related to an agricultural formulation comprising ethaboxam, metalaxyl and a compound selected from the group consisting of 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide and mandestrobin, a process for preparing the agricultural formulation and methods of use thereof.
Fungal infections are a major concern for crop growers. Fungi can be present on the seed surface prior to planting, they can be soil-borne, or they can be introduced into the growing environment by mobile pests or equipment. Fungi infect seeds and seedlings and destroy plant cells and tissues and thereby prevent seed germination or cause poor development or death of seedlings. Aphanomyces, Fusarium, Helminthosporium, Pythium, and Rhizoctonia are all known to cause infection and death of plants. These organisms cause seed rot, damping-off, seed blight, and root rot. Even diseases that affect adult plants can be controlled by pesticidal seed treatments (e.g., smuts caused by Ustilago, Tilletia, and Urocystis).
Metalaxyl is a widely used fungicide for controlling diseases among crops. Metalaxyl is the active ingredient in the seed treatment marketed as Sebring® 318 FS (Sebring is a registered trademark of and available from Nufarm Americas Inc) and Allegiance® FL. However, metalaxyl presents many formulations challenges including its low melting point (63-72° C.) and partial water solubility (8,400 parts per million). Liquid formulations of metalaxyl often form large crystals upon storage. Further, due to its low melting point, formulating metalaxyl with other low-melting point pesticides is highly problematic. To date there is no known finely milled aqueous slurry of metalaxyl and another low-melting point pesticide.
There remains a need in the art for physically and chemically stable formulations containing metalaxyl and other low-melting point pesticides useful for seed treatment that provides improved protection against fungal pests. Further, there is a need in the art for a process to prepare such physically and chemically stable formulations containing metalaxyl and other low-melting point pesticides.
The present invention is directed to an agricultural formulation comprising ethaboxam, metalaxyl, a compound selected from the group consisting of 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide and mandestrobin, propylene glycol, water, a colorant dispersant, a wetting agent selected from the group consisting of methyloxirane polymer, alkylphenol ethoxylate free nonionic wetter and polyoxyethylene tristyrylphenol phosphate, a sodium salt of naphthalene sulfonate condensate, a mixture of sodium salt of alkyl vinyl ether/maleic acid half-ester copolymer and polyvinyl pyrrolidone, and a silicone emulsion.
The present invention is further directed to a process for preparing an agricultural formulation comprising ethaboxam, metalaxyl and a compound selected from the group consisting of 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide and mandestrobin, comprising the steps of:
The present invention is further directed to an agricultural formulation comprising ethaboxam, metalaxyl and a compound selected from the group consisting of 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide and mandestrobin, produced by a process comprising the steps of:
The present invention is further directed to a method of protecting plants comprising treating plant propagation material with a fungicidally effective amount of an agricultural formulation of the present invention.
The present invention is further directed to a method for controlling or preventing pest damage of plants comprising applying to the plant propagation material an effective amount of an agricultural formulation of the present invention onto a plant propagation material.
The Applicant has discovered a stable agricultural formulation comprising ethaboxam, metalaxyl and a compound selected from the group consisting of 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide and mandestrobin can be produced. The Applicant has further discovered a process by which these agricultural formulations can be made. A stable agricultural formulation comprising ethaboxam, metalaxyl and a compound selected from the group consisting of 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide and mandestrobin is unexpected because of the co-melting that occurs between metalaxyl and other low-melting point actives. As previously mentioned, stable formulations containing metalaxyl are difficult to obtain because metalaxyl forms undesirable crystals. Applicants unexpectedly found that processes and formulations of the present invention provide a superior solution to this known problem in the art. Further, the agricultural formulation of the present invention is surprisingly stable when blended with NipsIt INSIDE®.
In one embodiment, the present invention is directed to an agricultural formulation comprising a compound selected from the group consisting of 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide and mandestrobin, preferably at a concentration from about 1% to about 10% w/w, ethaboxam, preferably at a concentration from about 1% to about 10% w/w, metalaxyl, preferably at a concentration from about 1% to about 5% w/w, propylene glycol, preferably at a concentration from about 10% to about 50% w/w, the wetting agent, preferably at a concentration from about 0.05% to about 10% w/w, a sodium salt of naphthalene sulfonate condensate, preferably at a concentration from about 0.1% to about 2% w/w, a mixture of sodium salt of alkyl vinyl ether/maleic acid half-ester copolymer and polyvinyl pyrrolidone, preferably at a concentration from about 0.01% to about 2% w/w, and a silicone emulsion, preferably at a concentration from about 0.01% to about 1% w/w. and optionally, xanthan gum, preferably at a concentration from about 0.01% to about 1% w/w and 1,2-benzisothiazolin-3-one prepared at a concentration of 19.3%, preferably at a concentration from about 0.01% to about 1% w/w, and optionally, a colorant, preferably at a concentration from about 1% to 30% w/w.
In another embodiment, the present invention is further directed to a process for preparing an agricultural formulation comprising ethaboxam, metalaxyl and a compound selected from the group consisting of 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide and mandestrobin, comprising the steps of:
In another embodiment, the present invention is further directed to an agricultural formulation comprising ethaboxam, metalaxyl and a compound selected from the group consisting of 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide and mandestrobin, produced by a process comprising the steps of:
bead milling ethaboxam and a compound selected from the group consisting of 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide and mandestrobin, to create a mill base;
In a preferred embodiment, the mill base comprises from about 1% to about 50% w/w ethaboxam, preferably about 15% to about 30% w/w and more preferably from about 19% to about 27% w/w and from about 1% to about 50% w/w of a compound selected from the group consisting of 3-(difluoromethyl)-1-methyl-N-[(3 R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide and mandestrobin, preferably about 15% to about 30% w/w and more preferably from about 18% to about 26% w/w.
In another preferred embodiment, the mill base comprises methyloxirane polymer, preferably at a concentration from about 0.1% to about 3% w/w, a sodium salt of naphthalene sulfonate condensate, preferably at a concentration from about 0.1% to about 2% w/w, a mixture of sodium salt of alkyl vinyl ether/maleic acid half-ester and polyvinyl pyrrolidone, preferably at a concentration from about 0.1% to about 1.1% w/w, a silicone emulsion, preferably at a concentration from about 0.01% to about 1.0% w/w, xanthan gum, preferably at a concentration from about 0.01% to about 1.0% w/w, 1,2-benzisothiazolin-3-one prepared at a concentration of 19.3%, preferably at a concentration from about 0.01% to about 1.0% w/w and water, preferably at a concentration from about 18% to about 98% w/w.
In another preferred embodiment, the metalaxyl solution comprises from about 1% to about 20% w/w metalaxyl and from about 80% to about 99% propylene glycol.
In another preferred embodiment, the agricultural formulation further comprises additional propylene glycol, preferably at a concentration from about 10% to about 20% w/w, a wetting agent selected from the additional methyloxirane polymer, an alkylphenol ethoxylate free nonionic wetter and polyoxyethylene tristyrylphenol phosphate, preferably the wetting agent is at a concentration from about 0.5% to about 5% w/w, a colorant dispersion and water.
In another preferred embodiment, the agricultural formulation further comprises additional mixture of sodium salt of alkyl vinyl ether/maleic acid half-ester copolymer and polyvinyl pyrrolidone, 25% carnauba wax emulsion, additional xanthan gum and additional 1,2-benzisothiazolin-3-one.
In another preferred embodiment, the agricultural formulation comprises from about 15% to about 35% w/w of the mill base and from about 10% to about 30% w/w of the metalaxyl solution.
In another preferred embodiment, the agricultural formulation further comprises clothianidin.
In another embodiment, the present invention is further directed to an agricultural formulation comprising:
In another embodiment, the present invention is further directed to an agricultural formulation comprising:
In another embodiment, the present invention is further directed to an agricultural formulation comprising:
In another embodiment, the present invention is further directed to a method of protecting plants comprising treating plant propagation material with a fungicidally effective amount of an agricultural formulation of the present invention.
In another embodiment, the present invention is further directed to a method for controlling or preventing pest damage of plants comprising applying to the plant propagation material an effective amount of an agricultural formulation of the present invention onto a plant propagation material.
As used herein, “plant propagation material” refers to seeds, bulbs, rhizomes and tubers.
In a preferred embodiment, the plant propagation material is a seed. In a more preferred embodiment, the formulations of the present invention are applied to the seeds before they are planted.
In another preferred embodiment, the plant that is treated is a crop plant. In a more preferred embodiment, the crop plant is selected from the group consisting of corn, soybeans, beans, peas, lentils, flax, wheat, rice, canola, sorghum, barley, oats, rye, millet and sugar beets.
The phrase “effective amount” of the formulation means a sufficient amount of the formulation to provide the desired effect. In general, the formulation is employed in amounts that do not inhibit germination of the seeds (or cause phytotoxic damage to the seeds) while providing adequate pest control. Pest control can mean reducing pest damage to the plant, reducing the amount of pests on the plant or in its immediate environment, or preventing the pests from reproducing, among other things. The amount of the formulation may vary depending on specific crops and other factors. It is well within the ordinary skill in the art to determine the necessary amount of the formulation.
As used herein, “pest” refers to pathogens and parasites that negatively affect the host plants by colonizing, attacking, irritating, or feeding upon them, or competing for nutrients with the host. A pest may be, for example, an undesirable bacterium, fungus including fungal pathogens, or insect.
Fungal pathogens include but are not limited to Rhizoctonia, Fusarium, Pythium Phytophthora, Phomopsis, and seed decay fungi including Aspergillus, Penicillium, Alternaria, Rhizopus, and Basidiomycete bunt and smut fungi.
As used herein, “plant” and “plants” refer to wild type and genetically modified members of the plant kingdom, including higher (vascular) plants and lower (non-vascular) plants.
As used herein, “crop plants” refers to cereal, legumes, forage crops, stem and leaf crops, tuber, bulb and root crops, fruit and seed vegetables, fruit and nut crops, beverage crops, oil, fat and wax crops, spices, perfumes and flavorings, and ornamentals, forest and fiber crops.
The formulations of the present invention may be applied simultaneous or sequentially to the areas in need of treatment.
The formulations of the present invention can be applied to any environment in need of pest control. The environment in need of pest control may include any area that is desired to have a reduced number of pests or to be free of pests. For example, the pesticide can be applied to areas where crop plants are grown.
As used herein, “controlling or preventing pest damage in a growing plant” refers to maintaining the population of the target pest at a rate per plant such that the plant is viable and produces an agriculturally useful product.
As used herein, all numerical values relating to amounts, weights, and the like, that are defined as “about” each particular value is plus or minus 10%. For example, the phrase “about 10% w/w” is to be understood as “9% w/w to 11% w/w.” Therefore, amounts within 10% of the claimed value are encompassed by the scope of the claims.
As used herein “% w/w” and “percent w/w” refer to the percent weight of the total formulation.
The disclosed embodiments are simply exemplary embodiments of the inventive concepts disclosed herein and should not be considered as limiting, unless the claims expressly state otherwise.
The following examples are intended to illustrate the present invention and to teach one of ordinary skill in the art how to use the formulations of the invention. They are not intended to be limiting in any way.
TABLE 1
Mill Base
% w/w
Ethaboxam
27.00
3-(difluoromethyl)-1-
18.00
methyl-N-[(3R)-
1,1,3-trimethyl-2,3-
dihydroinden-4-
yl]pyrazole-4-
carboxamide
Methyloxirane
0.25
polymer
Sodium salt of
1.00
naphthalene sulfonate
condensate
Mixture of sodium
0.25
salt of alkyl vinyl
ether/maleic acid
half-ester copolymer
and polyvinyl
pyrrolidone
Silicone emulsion
0.10
Xanthan gum
0.12
19.3% 1,2-
0.12
benzisothiazolin-3-
one
Water
53.16
TABLE 2
% w/w
1A
2A
3A
4A
5A
6A
7A
Mill base
25.818
25.818
25.818
25.818
25.818
25.818
25.818
10% Metalaxyl
20.091
20.091
20.091
20.091
20.091
20.091
20.091
Solution
Propylene Glycol
13.636
13.636
13.636
13.636
13.636
13.636
13.636
Alkylphenol
1.818
3.636
—
—
—
—
—
ethoxylate free
nonionic wetter
and dispersant
package
Methyloxirane
—
—
1.818
3.636
1.000
2.000
3.000
polymer
Colorant
20.182
20.182
20.182
20.182
20.182
20.182
20.182
Dispersion
Water
18.455
16.637
18.455
16.637
19.273
18.273
17.273
Ethaboxam TG was used as the source of ethaboxam and is available from Sumitomo Chemical.
3-(Difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide is available from Sumitomo Chemical.
Metalaxyl TG was used as the source for metalaxyl and is available from Nufarm Americas, Inc.
Pluronic® P-104 was used as the source of methyloxirane polymer (Pluronic is a registered trademark of and available from BASF Corporation).
Morwet® D-425 was used as the source of sodium salt of naphthalene sulfonate condensate (Morwet is a registered trademark of and available from Akzo Nobel Surface Chemistry LLC).
Easy-Sperse® P-20 was used as the source of mixture of sodium salt of alkyl vinyl ether/maleic acid half-ester copolymer and polyvinyl pyrrolidone (Easy-Sperse is a registered trademark of ISP Investments, Inc. and is available from Ashland).
Tersperse® 4894 was used as the source of alkylphenol ethoxylate free nonionic wetter and dispersant package (Tersperse is a registered trademark of and available from Huntsman Petrochemical Corporation).
Xiameter® AFE-0010 was used the source of silicone emulsion (Xiameter is a registered trademark of and available from Dow Corning Corporation).
Kelzan® CC was used as the source of xanthan gum (Kelzan is a registered trademark of and available from CP Kelco).
Proxel® GXL was used as the source of 19.3% 1,2-benzisothiazolin-3-one (Proxel is a registered trademark of Arch UK Biocides and is available from Lonza).
Treating Solutions™ Red 1048 was used as the source of colorant dispersion (Treating Solutions is a trademark of and available from Milliken & Company).
Method
Methyloxirane polymer, a sodium salt of naphthalene sulfonate condensate, a mixture of sodium salt of alkyl vinyl ether/maleic acid half-ester copolymer and polyvinyl pyrrolidone and a silicone emulsion were added to water under mechanical agitation until dissolved to create an excipient solution. 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide and ethaboxam were then dispersed in the excipient solution to create an active dispersion. The active solution was then milled with ceramic beads until the median particle diameter was less than 2.0 μm to achieve a milled suspension. Finally, an aqueous solution of xanthan gum and 19.3% 1,2-benzisothiazolin-3-one was added to the milled suspension to create a mill base. 20.8 grams of metalaxyl was dissolved in 200 grams of propylene glycol at 54° C. and then stirred to create a metalaxyl/propylene glycol solution. Alkylphenol ethoxylate free nonionic wetter and dispersant package or additional methyloxirane polymer was added to water under mechanical agitation until dissolved to create a surfactant solution. The surfactant solution was then added to the mill base while undergoing agitation. The rest of propylene glycol and the metalaxyl/propylene glycol solution were then added to the above-mentioned formulation followed by a colorant dispersion while undergoing agitation to create the final formulations.
Methods
Formulations 1A-7A from Table 2, above, were each separately subjected to 5 cycles of freeze thaw, 2 weeks at 54° C. and optionally, 4 weeks at 50° C. The physical properties of the Formulations 1A-4A are detailed in Table 3, below. Bottom clear time is the time until the formulation flows away from the container bottom when approximately 62.5 milliliters of the formulation is placed in a 125-milliliter plastic jar and placed on its side. Formulations 1A-4A were prepared as a small batch and 20 grams of each were stored in separate 30-milliliter glass vial. Formulations 5A-7A were prepared as a large batch and 70 grams of each were stored in a plastic jar. Chemical properties of Formulations 5A and 7A are detailed in Table 4, below.
TABLE 3
1A
2A
3A
4A
F/T
2 Weeks
F/T
2 Weeks
F/T
2 Weeks
F/T
2 Weeks
Initial
Cycle
54° C.
Initial
Cycle
54° C.
Initial
Cycle
54° C.
Initial
Cycle
54° C.
Syneresis %
n/a
0
10
n/a
0
15
n/a
0
4.6
n/a
0
6
Bottom
n/a
<1′
>26″
n/a
<1″
>8′
n/a
<1″
4′48″
n/a
<1″
13″
Clear Time
pH
7.36
7.33
7.28
7.35
7.23
7.11
7.60
7.53
7.34
7.55
7.49
7.34
Particle
1.60
1.42
2.11
1.45
1.56
1.62
1.46
1.46
1.46
1.54
1.68
2.70
Size
(d0.5 μm)
Viscosity
49.50
68.00
64.80
50.10
55.00
52.60
46.90
56.50
56.80
66.10
78.30
63.80
(50 s−1
mPa)
Sieve
n/a
0.014
0.15
n/a
0.007
0.066
n/a
0.015
0.014
n/a
0.065
0.02
Residue
(% > 150
μm)
5A
6A
7A
F/T
2 Weeks
4 Weeks
F/T
2 Weeks
4 Weeks
F/T
2 Weeks
4 Weeks
Initial
Cycle
54° C.
50° C.
Initial
Cycle
54° C.
50° C.
Initial
Cycle
54° C.
50° C.
Syneresis %
n/a
0
9.5
4.2
n/a
0
Trace
7.9
n/a
0
Trace
7.9
Bottom
n/a
<1″
>30′
>30′
n/a
<1″
10″
12″
n/a
<1″
10″
10″
Clear Time
pH
7.53
7.52
7.27
7.26
7.42
7.53
7.28
7.28
7.48
7.62
7.40
7.28
Particle
1.56
1.93
1.98
1.83
1.54
1.70
1.62
1.57
1.52
1.81
1.53
1.49
Size
(d0.5 μm)
Viscosity
38.70
70.90
72.50
63.00
42.10
61.90
60.60
60.60
46.60
65.90
61.00
64.10
(50 s−1
mPa)
Sieve
n/a
0.002
0.003
0.003
n/a
0.003
0.001
0.004
n/a
0.003
0.001
0.004
Residue
(% > 150
μm)
TABLE 4
5A
7A
2 Weeks
4 Weeks
2 Weeks
4 Weeks
% w/w
Initial
F/T Cycle
54° C.
50° C.
Initial
F/T Cycle
54° C.
50° C.
Ethaboxam
7.03
6.84
6.77
6.73
6.96
6.96
6.87
6.83
3-(difluoromethyl)-1-
4.71
4.60
4.62
4.61
4.69
4.55
4.57
4.60
methyl-N-[(3R)-1,1,3-
trimethyl-2,3-
dihydroinden-4-
yl]pyrazole-4-
carboxamide
Metalaxyl
1.94
1.95
1.95
1.93
1.97
1.95
1.95
1.96
Results
As can be seen in Tables 3 and 4, formulations of the present invention are physically and chemically stable following accelerated storage testing.
Methods
Formulations 1A-7A from Table 2, above, were each blended with Nipslt INSIDE® (Nipslt INSIDE is a registered trademark of and available from Valent U.S.A. LLC) at approximately 1:1 ratio, and separately subjected to 5 cycles of freeze thaw, 2 weeks at 54° C. and optionally, 4 weeks at 40° C. The physical properties of the final formulations are detailed in Table 5, below.
TABLE 5
1A + NipsIt INSIDE ®
2A + NipsIt INSIDE ®
2 Weeks
2 Weeks
Initial
F/T Cycle
54° C.
Initial
F/T Cycle
54° C.
Syneresis %
n/a
4.9
7.4
n/a
4.9
7.4
Bottom Clear Time
n/a
1′18″
12″
n/a
11″
12″
pH
7.11
7.09
7.02
7.04
6.89
6.97
Particle Size
1.29
1.66
1.70
1.57
1.92
1.76
(d0.5 μm)
Viscosity
74.10
88.60
78.90
84.50
105.00
85.00
(50 s−1 mPa)
Sieve Residue
n/a
0.017
0.021
n/a
0.02
0.023
(% > 150 μm)
3A + NipsIt INSIDE ®
4A + NipsIt INSIDE ®
2 Weeks
2 Weeks
Initial
F/T Cycle
54° C.
Initial
F/T Cycle
54° C.
Syneresis %
n/a
4.9
7.3
n/a
4.9
5
Bottom Clear Time
n/a
103″
12″
n/a
15″
12″
pH
7.25
7.06
7.20
7.19
7.01
7.16
Particle Size
1.51
1.98
1.67
1.64
2.02
1.61
(d0.5 μm)
Viscosity
82.40
102.00
83.00
95.70
110.00
95.50
(50 s−1 mPa)
Sieve Residue
n/a
0.023
0.033
n/a
0.029
0.045
(% > 150 μm)
5A + NipsIt INSIDE ®
6A + NipsIt INSIDE ®
2 Weeks
4 Weeks
2 Weeks
4 Weeks
Initial
F/T Cycle
54° C.
40° C.
Initial
F/T Cycle
54° C.
40° C.
Syneresis %
n/a
5.7
13
9.9
n/a
7.3
10
9.3
Bottom Clear Time
n/a
9″
20″
40″
n/a
9″
20″
1′40″
pH
7.18
7.19
7.21
6.88
7.06
7.08
7.25
6.84
Particle Size
1.58
1.88
1.59
1.72
1.58
1.88
1.67
1.66
(d0.5 μm)
Viscosity
74.60
91.50
77.90
93.50
75.50
95.60
79.90
111.00
(50 s−1 mPa)
Sieve Residue
n/a
0.013
0.002
0.003
n/a
0.007
0.003
0.003
(% > 150 μm)
7A + NipsIt INSIDE ®
2 Weeks
4 Weeks
Initial
F/T Cycle
54° C.
40° C.
Syneresis %
n/a
8.5
13
14
Bottom Clear Time
n/a
9″
20″
3′20″
pH
7.16
7.13
7.27
6.89
Particle Size
1.59
1.89
1.65
1.52
(d0.5 μm)
Viscosity
77.10
97.10
80.90
90.70
(50 s−1 mPa)
Sieve Residue
n/a
0.010
0.006
0.005
(% > 150 μm)
Results
As can be seen in Table 5, formulations of the present invention blended with Nipslt INSIDE® are physically stable following accelerated storage testing.
TABLE 6
Mill Base
% w/w
Ethaboxam
27.00
3-(difluoromethyl)-1-methyl-N-[(3R)-
18.00
1,1,3-trimethyl-2,3-dihydroinden-4-
yl]pyrazole-4-carboxamide
Methyloxirane polymer
0.25
Sodium salt of naphthalene sulfonate
1.00
condensate
Mixture of sodium salt of alkyl vinyl
0.25
ether/maleic acid half-ester copolymer
and polyvinyl pyrrolidone
Silicone emulsion
0.10
Xanthan gum
0.12
19.3% 1,2-benzisothiazolin-3-one
0.12
Water
53.16
TABLE 7
% w/w
8A
8B
9A
10A
Mill base
19.72
19.72
19.72
19.72
10% Metalaxyl Solution
28.43
28.43
28.43
28.43
Propylene Glycol
17.41
17.41
17.41
17.36
Mixture of sodium salt of alkyl
0.46
0.46
0.65
0.46
vinyl ether/maleic acid half-
ester copolymer and polyvinyl
pyrrolidone
Methyloxirane polymer
1.85
1.85
1.85
2.46
Xanthan gum
0.097
0.097
0.097
0.097
19.3% 1,2-benzisothiazolin-3-
0.097
0.217
0.097
0.097
one
Colorant Dispersion
15.46
15.46
15.46
15.46
Water
16.476
16.356
16.286
15.916
Ethaboxam TG was used as the source of ethaboxam and is available from Sumitomo Chemical.
3-(Difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide is available from Sumitomo Chemical.
Metalaxyl TG was used as the source for metalaxyl and is available from Nufarm Americas, Inc.
Pluronic® P-104 was used as the source of methyloxirane polymer.
Morwet® D-425 was used as the source of sodium salt of naphthalene sulfonate condensate.
Easy-Sperse® P-20 was used as the source of mixture of sodium salt of alkyl vinyl ether/maleic acid half-ester copolymer and polyvinyl pyrrolidone.
Xiameter® AFE-0010 was used the source of silicone emulsion.
Kelzan® CC was used as the source of xanthan gum.
Proxel® GXL was used as the source of 19.3% 1,2-benzisothiazolin-3-one.
Treating Solutions™ Red 1048 was used as the source of colorant dispersion.
Method
Methyloxirane polymer, a sodium salt of naphthalene sulfonate condensate, a mixture of sodium salt of alkyl vinyl ether/maleic acid half-ester copolymer and polyvinyl pyrrolidone and a silicone emulsion were added to water under mechanical agitation until dissolved to create an excipient solution. 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide and ethaboxam were then dispersed in the excipient solution to create an active dispersion. The active dispersion was then milled with ceramic beads until the median particle diameter was less than 2.0 μm to achieve a milled suspension. Finally, an aqueous solution of xanthan gum and 19.3% 1,2-benzisothiazolin-3-one was added to the milled suspension to create a mill base. 20.8 grams of metalaxyl was dissolved in 179.2 grams of propylene glycol at 54° C. and then stirred to create a metalaxyl/propylene glycol solution. Additional methyloxirane polymer was heated at 54° C. and added to propylene glycol under mechanical agitation until dissolved to create a surfactant solution. Additional aqueous solution of xanthan gum and 19.3% 1,2-benzisothiazolin-3-one, additional amount of a mixture of sodium salt of alkyl vinyl ether/maleic acid half-ester copolymer and polyvinyl pyrrolidone, the surfactant solution, propylene glycol, the metalaxyl solution, and a colorant dispersion were then added to the mill base while undergoing agitation to create the final formulations.
Methods
Formulations 8A-10A from Table 7, above, were each separately subjected to 5 cycles of freeze thaw and 4 weeks at 50° C. The physical properties of the Formulations 8A-10A are detailed in Table 8, below. Bottom clear time is the time until the formulation flows away from the container bottom when approximately 62.5 milliliters of the formulation is placed in a 125-milliliter plastic jar and placed on its side. Chemical properties of Formulations 8A-10A are detailed in Table 9, below.
TABLE 8
8A
9A
10A
4 Weeks
4 Weeks
4 Weeks
Initial
F/T Cycle
50° C.
Initial
F/T Cycle
50° C.
Initial
F/T Cycle
50° C.
Syneresis %
n/a
0
trace
n/a
0
0
n/a
0
0
Bottom Clear Time
n/a
1″
10″
n/a
1″
10″
n/a
1″
8″
pH
7.39
7.43
7.23
7.16
7.20
7.02
7.39
7.41
7.18
Particle
1.61
1.80
1.38
1.52
1.86
1.43
1.55
1.81
1.36
Size
(d0.5 μm)
Viscosity
125.9
135.5
174.3
117.7
140.3
177.8
115.1
144.3
156.0
(50 s−1
mPa)
Sieve
n/a
0.001
0.001
n/a
0.001
0.002
n/a
0.001
0.002
Residue
(% > 150 μm)
TABLE 9
8A
9A
10A
4 Weeks
4 Weeks
4 Weeks
% w/w
Initial
F/T Cycle
50° C.
Initial
F/T Cycle
50° C.
Initial
F/T Cycle
50° C.
Ethaboxam
5.20
5.23
5.18
5.21
5.18
5.14
5.13
5.10
5.08
3-(difluoromethyl)-1-
3.48
3.48
3.46
3.46
3.48
3.46
3.49
3.49
3.45
methyl-N-[(3R)-1,1,3-
trimethyl-2,3-
dihydroinden-4-
yl]pyrazole-4-
carboxamide
Metalaxyl
2.84
2.84
2.83
2.82
2.82
2.81
2.82
2.83
2.83
Results
As can be seen in Tables 8 and 9, formulations of the present invention are physically and chemically stable following accelerated storage testing.
Methods
Formulations 8A-10A from Table 7, above, were each blended with Nipslt INSIDE® at 57:43 ratio, and separately subjected to 5 cycles of freeze thaw and 4 weeks at 50° C. The physical properties of the final formulations are detailed in Table 10, below.
TABLE 10
8A + NipsIt INSIDE ®
9A + NipsIt INSIDE ®
10A + NipsIt INSIDE ®
4 Weeks
4 Weeks
4 Weeks
Initial
F/T Cycle
50° C.
Initial
F/T Cycle
50° C.
Initial
F/T Cycle
50° C.
Syneresis %
n/a
Trace
Trace
n/a
Trace
Trace
n/a
Trace
Trace
Bottom Clear Time
n/a
1″
15″
n/a
1″
12″
n/a
1″
12″
pH
7.29
7.20
6.63
7.09
7.04
6.56
7.24
7.13
6.60
Particle Size
1.68
2.00
2.22
1.69
1.89
2.66
1.70
1.84
2.29
(d0.5 μm)
Viscosity
126.0
156.7
200.4
128.3
155.7
201.9
129.0
154.6
185.1
(50 s−1 mPa)
Sieve Residue
n/a
0.032
0.032
n/a
0.027
0.032
n/a
0.031
0.033
(% > 150 μm)
Results
As can be seen in Table 10, formulations of the present invention blended with Nipslt INSIDE® are physically stable following accelerated storage testing.
TABLE 11
Ingredient
11A
12A
13A
14A
15A
Ethaboxam
2.38
2.38
2.35
2.35
2.35
Metalaxyl
1.27
1.27
1.25
1.25
1.25
Mandestrobin
3.17
3.17
3.13
3.13
3.13
Methyloxirane
0.065
0.065
0.065
0.065
0.065
polymer
Sodium salt of
0.262
0.262
1.262
1.262
0.262
naphthalene sulfonate
condensate
Mixture of sodium
0.065
1.065
0.065
0.065
0.065
salt of alkyl vinyl
ether/maleic acid
half-ester copolymer
and polyvinyl
pyrrolidone
Alkylphenol
1.0
—
1.0
—
—
ethoxylate free
nonionic wetter and
dispersant package
Polyoxyethylene
—
—
1.0
3.0
3.0
tristyrylphenol
phosphate, potassium
salt
Colorant dispersion
—
—
7.33
7.33
7.33
19.3% 1,2-
0.24
0.24
0.24
0.24
0.24
benzisothiazolin-3-
one
Carnauba wax, 25%
2.5
2.5
2.5
2.5
2.5
emulsion
Silicone emulsion
0.026
0.026
0.026
0.026
0.026
Xanthan gum
0.3
0.151
0.3
0.3
0.3
Propylene glycol
35.381
35.441
34.041
34.041
34.041
Water
Q.S.
Q.S.
Q.S.
Q.S.
Q.S.
Stepfac™ TSP PE-K (CAS #163436-84-8) is polyoxyethylene tristyrylphenol phosphate, potassium salt and is available from Stepan Corp.
Michem® Lube 156P (CAS# proprietary) is used as the source of carnauba wax (25% emulsion in water) and is a registered trademark of and available from Michelman Inc.
Agrocer® Red 112 is used as the source of colorant dispersion and is a registered trademark and available from Clariant AG.
Method
Methyloxirane polymer, a sodium salt of naphthalene sulfonate condensate, a mixture of sodium salt of alkyl vinyl ether/maleic acid half-ester copolymer and polyvinyl pyrrolidone and a silicone emulsion were added to water under mechanical agitation until dissolved to create an excipient solution. Mandestrobin and ethaboxam were then dispersed in the excipient solution to create an active dispersion. The active solution was then milled with ceramic beads until the median particle diameter was less than 2.0 μm to achieve a milled suspension. Finally, an aqueous solution of xanthan gum and 19.3% 1,2-benzisothiazolin-3-one was added to the milled suspension to create a mill base. 20.8 grams of metalaxyl was dissolved in 179.2 grams of propylene glycol at 54° C. and then stirred to create a metalaxyl/propylene glycol solution. Additional aqueous solution of xanthan gum and 19.3% 1,2-benzisothiazolin-3-one, either alkylphenol ethoxylate free nonionic wetter and dispersant package or additional amount of a mixture of sodium salt of alkyl vinyl ether/maleic acid half-ester copolymer and polyvinyl pyrrolidone, 25% carnauba wax emulsion, the rest of propylene glycol, and the metalaxyl solution were then added to the mill base while undergoing agitation to create the final formulations.
Formulations 11A and 12A from Table 11, above, were each separately subjected to 5 cycles of freeze thaw, 2 weeks at 54° C. and 4 and 8 weeks at 50° C. The physical properties of the Formulations 11A and 12A are detailed in Table 12, below. Bottom clear time is the time until the formulation flows away from the container bottom when approximately 62.5 milliliters of the formulation is placed in a 125-milliliter plastic jar and placed on its side. Formulations 11A and 12A were prepared as a small batch and 20 grams of each were stored in separate 30-milliliter glass vial.
TABLE 12
11A
12A
2
4
8
2
4
8
F/T
Weeks
Weeks
Weeks
F/T
Weeks
Weeks
Weeks
Initial
Cycle
54° C.
50° C.
50° C.
Initial
Cycle
54° C.
50° C.
50° C.
Syner-
—
0
2.97%
9.43%
30.77%
—
7.50%
9.21%
9.30%
13.30%
esis
%
Bottom
—
1 s
1 s
1 s
1 s
—
1 s
1 s
1 s
1 s
Clear
Time
Spray-
0.000%
0.000%
0.000%
0.000%
0.006%
0.000%
0.003%
0.000%
0.003%
0.003%
ability
pH
6.88
6.66
6.37
6.42
5.91
6.08
5.97
5.50
5.54
5.32
Vis-
1860
1985
2047
20.18
2075
1333
1352
1569
1477
1385
cosity
(1 s−1
mPa)
Vis-
117.5
126.8
134.3
132.9
135.4
99.09
103.6
125.6
115.8
111.4
cosity
(50 s−1
mPa)
G′
3.985
4.232
4.613
4.517
4.38
2.582
2.711
3.083
2.962
2.666
(t = 0.1
Pa)
G″
2.257
2.405
2.615
2.568
2.607
1.779
1.848
2.114
2.039
1.979
(t = 0.1
Pa)
G′/G″
1.77
1.76
1.76
1.76
1.68
1.45
1.47
1.46
1.45
1.35
ratio
TABLE 13
13A
14A
2 Weeks
4 Weeks
8 Weeks
2 Weeks
Initial
F/T Cycle
54° C.
50° C.
50° C.
F/T Cycle
54° C.
Syneresis %
—
0.00%
0.00%
6.67%
0.15%
0.00%
0.00%
Bottom Clear Time
—
1 s
2 s
1 s
3 s
1 s
1 s
Sprayability
0.00%
0.00%
0.00%
0.00%
0.003%
0.00%
0.00%
pH
6.46
6.47
5.81
—
6.77
7.79
7.45
Viscosity
2183
2234
2616
4410
4389
2353
2650
(1 s−1 mPa)
Viscosity
138.2
146.3
161.3
152
197.5
149.7
163.2
(50 s−1 mPa)
G′ (t = 0.1
5.264
5.551
6.171
15.1
22.05
5.329
5.903
Pa)
G″ (t = 0.1
2.835
2.949
3.198
3.466
4.606
2.912
3.163
Pa)
G′/G″ ratio
1.86
1.88
1.93
4.36
4.79
1.83
1.87
15A
2 Weeks
4 Weeks
8 Weeks
Initial
F/T Cycle
54° C.
50° C.
50° C.
Syneresis %
—
2.70%
5.63%
—
0.06%
Bottom Clear Time
—
1 s
1 s
—
8s
Sprayability
0.00%
0.00%
0.00%
0.001%
0.004%
pH
6.55
6.53
6.16
—
7.46
Viscosity
2332
23.5
2380
3487
3167
(1 s−1 mPa)
Viscosity
142.4
142.3
150.5
140.3
150.2
(50 s−1 mPa)
G′ (t = 0.1 Pa)
5.277
5.202
5.399
8.994
5.552
G″ (t = 0.1 Pa)
2.883
2.854
2.969
2.923
2.967
G′/G″ ratio
1.83
1.82
1.82
3.08
1.87
Results
As can be seen in Tables 12 and 13, formulations of the present invention are physically stable following accelerated storage testing.
Zhou, Ke, Ogawa, Toshiya, Tanuwidjaja, Jessica
| Patent | Priority | Assignee | Title |
| Patent | Priority | Assignee | Title |
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